FDA.reportPublic FDA data

NDC 13985-575 - ThyroVet Equine

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
13985-575
Package NDCs from labels
13985-575-01, 13985-575-10
Manufacturer
MWI/Vet One | First Priority Incorporated
Effective date
2023-11-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
ThyroVet Equine - MWI/Vet One | First Priority IncorporatedMWI/Vet One | First Priority Incorporated2023-11-07PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
13985-575-01ThyroVetEquine12 in 1 CASEPOWDER125
13985-575-01ThyroVetEquine453.6 g in 1 JARPOWDER453.65
13985-575-10ThyroVetEquine1 in 1 CASEPOWDER15
13985-575-10ThyroVetEquine453600 g in 1 PAILPOWDER4536005

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
13985-575THYROVET EQUINE (LEVOTHYROXINE SODIUM) POWDER [MWI/VET ONE]54 package rows20231108_63704bc7-bf94-44c1-b1c7-2bfbbaed327b.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 14 of 14 · 270 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Levothyroxine SodiumLEVOTHYROXINE SODIUMFresenius Kabi USA, LLC388a1f15-8c1c-46a5-997f-7f326f696b592020-12-04Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 9J765S329G
Levothyroxine SodiumLEVOTHYROXINE SODIUMFresenius Kabi USA, LLC50b1c8a4-75b6-49c8-80fc-3841ee80b1832020-12-04Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 9J765S329G
levothyroxine sodiumLEVOTHYROXINE SODIUMProficient Rx LP12ccf2fd-ccf0-4bcf-8eee-e2a16c8b44d62020-12-01Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 9J765S329G
Levothyroxine SodiumLEVOTHYROXINE SODIUMProficient Rx LP97e28b00-9913-463f-9de2-08c828edbe672020-03-01Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 9J765S329G
Levothyroxine SodiumLEVOTHYROXINE SODIUMProficient Rx LP05ab038e-45fa-488e-a05e-12a2dd3564c12020-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 9J765S329G
Levothyroxine SodiumLEVOTHYROXINE SODIUMProficient Rx LPb81720f9-2836-4c1d-8691-0f6acef133162020-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 9J765S329G
levothyroxine sodiumLEVOTHYROXINE SODIUMProficient Rx LP3019762c-d480-4530-a3b2-762b523e79612019-11-01Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 9J765S329G
Levothyroxine SodiumLEVOTHYROXINE SODIUMProficient Rx LP434075d5-a82b-4f17-85e6-4c1922663dbc2019-10-01Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 9J765S329G
Levothyroxine SodiumLEVOTHYROXINE SODIUMProficient Rx LP18c7c63a-642e-47fe-a8ee-12aaf652b2aa2019-10-01Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 9J765S329G
UnithroidLEVOTHYROXINE SODIUMAmneal Pharmaceuticals LLC07562e72-7eaa-4ce6-94f0-e08814787e502019-06-19Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 9J765S329G

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.